American Hospital Association

FDA issues most serious recall for certain pacemaker devices by Boston Scientific

The Food and Drug Administration has issued a Class I recall correction for certain Boston Scientific ACCOLADE pacemakers and cardiac resynchronization therapy pacemakers after identifying a software- ...
Healio

Leadless conduction system pacemaker works, but dislodgement issues spur redesign

A novel leadless pacemaker designed for left bundle branch area pacing conferred successful pacing parameters at 1 month, but ...
Becker's Hospital Review

Boston Scientific recalls pacemakers after 4 deaths, 2,500 injuries

Boston Scientific recalls pacemakers due to battery issues causing safety mode activation linked to 4 deaths and 2,557 serious injuries, FDA reports.
WATE 6 On Your Side

FDA issues recall on pacemakers; Hackers could turn off devices

SILVER SPRING, MD (WCMH) — The FDA is issuing a major recall, saying that half a million people’s pacemakers could be hacked. The Food and Drug Administration discovered flaws that could allow a ...
Hosted on MSN

Recalls widen to pacemakers, food, and consumer goods

Pacemaker safety recall: FDA recalled certain Boston Scientific pacemakers due to a software flaw linked to deaths and serious injuries, advising in-clinic software updates. Widespread Salmonella risk ...
Hosted on MSN

FDA issues highest-risk recall for Boston Scientific pacemakers

Highest-risk classification: FDA labeled Boston Scientific’s pacemaker recall as Class I, the most serious, due to potential ...